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rs786201912

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201912(C;T)
Make rs786201912(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214792363
GeneBARD1
is asnp
is mentioned by
dbSNPrs786201912
ebirs786201912
HLIrs786201912
Exacrs786201912
Varsomers786201912
Maprs786201912
PheGenIrs786201912
hapmaprs786201912
1000 genomesrs786201912
hgdprs786201912
ensemblrs786201912
gopubmedrs786201912
geneviewrs786201912
scholarrs786201912
googlers786201912
pharmgkbrs786201912
gwascentralrs786201912
openSNPrs786201912
23andMers786201912
23andMe allrs786201912
SNP Nexus

SNPshotrs786201912
SNPdbers786201912
MSV3drs786201912
GWAS Ctlgrs786201912
Max Magnitude0
ClinVar
Risk rs786201912(T;T)
Alt rs786201912(T;T)
Reference rs786201912(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215657087G>A
CLNSRC
CLNACC RCV000164438.1,